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Role of artificial intelligence in developing predictive models for major adverse cardiovascular outcomes using CCTA

Sadaf Salehi1, Seyed Hesam Hojjat2, Ali Samadi Shams3

  • 1Student Research Committee, Iran University of Medical Sciences, Tehran, Iran.

Insights

Artificial intelligence models using coronary CT angiography-derived fat imaging show promise for predicting major adverse cardiovascular events (MACEs). Deep learning approaches offer superior accuracy, but more standardization is needed for clinical use.

Area of Science:

  • Cardiovascular Imaging
  • Artificial Intelligence in Medicine
  • Radiomics

Background:

  • Cardiovascular diseases are a leading global cause of death.
  • Accurate risk stratification for major adverse cardiovascular events (MACEs) is crucial.
  • Coronary computed tomography angiography (CCTA) and its radiomic features show potential for MACE prediction.

Purpose of the Study:

  • To systematically review and meta-analyze the predictive performance of AI-driven models using CCTA-derived adipose tissue radiomic features for MACE forecasting.
  • To compare the efficacy of different AI algorithms in predicting MACEs.

Main Methods:

  • Systematic review and random-effects meta-analysis following PRISMA guidelines.
  • Inclusion of 11 studies with 47,244 participants evaluating AI models utilizing CCTA-derived adipose tissue radiomics for MACE prediction.
  • Performance assessment using pooled area under the receiver operating characteristic curve (AUC), sensitivity, and specificity.

Main Results:

  • AI models integrating CCTA radiomics and clinical data showed pooled AUCs from 82.2% to 87.9%, outperforming conventional tools.
  • Deep learning models exhibited superior predictive performance compared to traditional machine learning and logistic regression.
  • Significant heterogeneity (I² > 96%) was noted across studies.

Conclusions:

  • AI-enhanced CCTA adipose tissue characterization holds significant potential for improving MACE risk prediction.
  • Methodological heterogeneity and limited external validation currently hinder widespread clinical application.
  • Future research requires standardized methods, rigorous validation, and transparent reporting for clinical integration.

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